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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K911400
 
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Product Description
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FDA Recall
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MicroScan WalkAway-40 plus Instrument REF B1018-283 2 05/13/2022 Beckman Coulter Inc.
MicroScan WalkAway-40 plus Reconditioned Instrument REF B1018-340R 2 05/13/2022 Beckman Coulter Inc.
DxM 1096 MicroScan WalkAway Instrument REF B1018-496 2 05/13/2022 Beckman Coulter Inc.
DxM 1040 MicroScan WalkAway Instrument REF B1018-440 2 05/13/2022 Beckman Coulter Inc.
MicroScan WalkAway-96 plus Instrument REF B1018-284 2 05/13/2022 Beckman Coulter Inc.
MicroScan WalkAway-96 plus Reconditioned Instrument REF B1018-396R 2 05/13/2022 Beckman Coulter Inc.
MicroScan WalkAway-96 plus Reconditioned Instrument 2 04/07/2021 Beckman Coulter Inc.
MicroScan WalkAway-40 plus Reconditioned Instrument 2 04/07/2021 Beckman Coulter Inc.
MicroScan WalkAway-96 plus Instrument 2 04/07/2021 Beckman Coulter Inc.
MicroScan WalkAway-40 plus Instrument 2 04/07/2021 Beckman Coulter Inc.
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